MECP2 mutation in male patients with non-specific X-linked mental retardation

FEBS Letters

Volumn 481, Issue 3, 2000, Pages 285-288

  Orrico, Alfredo ^a   Lam, Ching Wan ^b   Galli, Lucia ^a   Dotti, Maria Teresa ^c   Hayek, Giuseppe ^a   Tong, Sui Fan ^b   Poon, Priscilla M K ^b   Zappella, Michele ^a   Federico, Antonio ^c   Sorrentino, Vincenzo ^a,c,d  

^a UNIVERSITY HOSPITAL OF SIENA   (Italy)

^b CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

^c UNIVERSITY OF SIENA   (Italy)

^d SAN RAFFAELE HOSPITAL   (Italy)

Author keywords

Development; MECP2 gene; Missense mutation; X linked mental retardation

Indexed keywords

BINDING PROTEIN; DNA; PROTEIN MECP2; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CHROMOSOME XQ; CONTROLLED STUDY; CPG ISLAND; DNA SEQUENCE; FEMALE; GENE SEGREGATION; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; MENTAL DEFICIENCY; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RETT SYNDROME; SCHOOL CHILD; X CHROMOSOME LINKED DISORDER;

ADULT; AUTISTIC DISORDER; CASE REPORT; CHILD; CHILD, PRESCHOOL; DNA-BINDING PROTEINS; FEMALE; HUMAN; LINKAGE (GENETICS); MALE; MENTAL RETARDATION; MIDDLE AGE; MUTATION, MISSENSE; PEDIGREE; REPRESSOR PROTEINS; RETT SYNDROME; SEX FACTORS; SUPPORT, NON-U.S. GOV'T; X CHROMOSOME;

EID: 18244432131     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-5793(00)01994-3     Document Type: Article

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